Nara F, Matsuyama S, Mizuno T, Mizushima S
Mol Gen Genet. 1986 Feb;202(2):194-9. doi: 10.1007/BF00331636.
Expression of the ompF and ompC genes coding for major outer membrane proteins is osmoregulated by solutes, such as sucrose and NaCl, in the growth medium. The OmpR protein, a positive regulator of these genes, is involved in the osmoregulation (Dairi et al. 1985; Nara et al. 1984). In the present work, five mutant ompR genes exhibiting different phenotypes of osmoregulation were cloned and sequenced. Three of them, ompR1, ompR2 and ompR20, were previously isolated mutants. The others, ompR3 and ompR4, were isolated in the present work. The ompR1 mutation resulted in the deletion of 19 amino acids near the C-terminus of the OmpR protein. The ompR3 and ompR4 mutations resulted in Arg15 to Cys and Arg71 to Thr conversions, respectively, at the N-terminal portion, whereas the ompR20 and ompR2 mutations resulted in Arg150 to Cys and Val207 to Met conversions, respectively, at the C-terminal portion. Based on these results, the structure and function of the OmpR protein are discussed in relation to the mechanism of osmoregulation.
编码主要外膜蛋白的ompF和ompC基因的表达受生长培养基中的溶质(如蔗糖和氯化钠)的渗透调节。OmpR蛋白是这些基因的正调控因子,参与渗透调节(Dairi等人,1985年;Nara等人,1984年)。在本研究中,克隆并测序了五个表现出不同渗透调节表型的ompR突变基因。其中三个,ompR1、ompR2和ompR20,是先前分离的突变体。另外两个,ompR3和ompR4,是在本研究中分离得到的。ompR1突变导致OmpR蛋白C末端附近缺失19个氨基酸。ompR3和ompR4突变分别导致N末端部分的Arg15转换为Cys和Arg71转换为Thr,而ompR20和ompR2突变分别导致C末端部分的Arg150转换为Cys和Val207转换为Met。基于这些结果,结合渗透调节机制对OmpR蛋白的结构和功能进行了讨论。